A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581242



Internal ID20954313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67095709..67096323hg38UCSC Ensembl
chr16:67129612..67130226hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2908n223
Supporting Variantsnssv18243600
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581242
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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